Canonical Allele Identifier: PA2826816383
Gene: WWOX HGNC NCBI

Linked Data

ClinVar Variation Id: 506528
ClinVar RCV Id: RCV000650211 RCV001722560 RCV001815005
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001278926.1:p.Gly297Cys
CA8183802
NM_001291997.2:c.889G>T